Variant report

Variant	rs72735731
Chromosome Location	chr4:148091915-148091916
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10002243	0.85[EUR][1000 genomes]
rs10010037	0.85[EUR][1000 genomes]
rs10010117	0.85[EUR][1000 genomes]
rs10012343	0.85[EUR][1000 genomes]
rs10034616	0.85[EUR][1000 genomes]
rs10155125	0.93[EUR][1000 genomes]
rs72733798	0.85[EUR][1000 genomes]
rs72735715	0.85[EUR][1000 genomes]
rs72735721	0.84[EUR][1000 genomes]
rs72735726	1.00[EUR][1000 genomes]
rs72735733	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7677110	0.85[EUR][1000 genomes]
rs7697358	0.85[EUR][1000 genomes]
rs7698560	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024629	chr4:147987351-148277008	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148090800-148092400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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